Polyposis syndromes– what to do when genotyping seems not informative

by Macrae F
Published 2012-04-01

When is it best to test? Attitudes of health professionals regarding genetic testing for Familial Adenomatous Polyposis (FAP)

by Lynch E, Duncan RE, Macrae F, Delatycki M
Published 2012-04-01

Prevalence of mental health disorders in inflammatory bowel disease: an Australian outpatient cohort

by Tribbick D, Salzberg M, Ftanou M, Connell WR, Macrae F, Kamm MA, Bates GW, Cunningham G, Austin DW, Knowles SR
Published 2015-07-01

Audit of routine immunohistochemistry testing for mismatch repair proteins at diagnosis of colorectal cancer under the age of 50

by Lipton L, Kentwell M, Li M, Williams D, Christie M, Landgren A, Dow C, Jones I, McLaughlin S, Delatycki M, Macrae F, Lynch E
Published 2012-04-01

Angiotensin-induced abdominal aortic aneurysms in hypercholesterolemic mice: role of serum cholesterol and temporal effects of exposure.

by Petra A Prins, Michael F Hill, David Airey, Sam Nwosu, Prudhvidhar R Perati, Hagai Tavori, Macrae F Linton, Valentina Kon, Sergio Fazio, Uchechukwu K Sampson
Published 2014-01-01

The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease

by Savige, J., Dalgleish, R., Cotton, R.G.H., Dunnen, J.T. den, Macrae, F., Povey, S.
Published 2015

The tribes on my frontier; an Indian naturalist's foreign policy,

by Aitken, Edward Hamilton, 1851-1909., Macrae, F. C. ill
Published 1892

The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome

by Plazzer, J.P., Sijmons, R.H., Woods, M.O., Peltomaki, P., Thompson, B., Dunnen, J.T. den, Macrae, F.
Published 2013

Mutation (variation) databases and registries: a rationale for coordination of efforts

by Auerbach, A.D., Burn, J., Cassiman, J.J., Claustres, M., Cotton, R.G.H., Cutting, G., Dunnen, J.T. den, El-Ruby, M., Vargas, A.F., Greenblatt, M.S., Macrae, F., Matsubara, Y., Rimoin, D.L., Vihinen, M., Broeckhoven, C. van, Human Variome Project
Published 2011

Deciphering the Colon Cancer Genes-Report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010

by Kohonen-Corish, M.R.J., Macrae, F., Genuardi, M., Aretz, S., Bapat, B., Bernstein, I.T., Burn, J., Cotton, R.G.H., Dunnen, J.T. den, Frebourg, T., Greenblatt, M.S., Hofstra, R., Holinski-Feder, E., Lappalainen, I., Lindblom, A., Maglott, D., Moller, P., Morreau, H., Moslein, G., Sijmons, R., Spurdle, A.B., Tavtigian, S., Tops, C.M.J., Weber, T.K., Wind, N. de, Woods, M.O., Contributors InSiGHT-HVP Workshop
Published 2011

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

by Movahedi, M., Bishop, D.T., Macrae, F., Mecklin, J.P., Moeslein, G., Olschwang, S., Eccles, D., Evans, D.G., Maher, E.R., Bertario, L., Bisgaard, M.L., Dunlop, M.G., Ho, J.W., Hodgson, S.V., Lindblom, A., Lubinski, J., Morrison, P.J., Murday, V., Ramesar, R.S., Side, L., Scott, R.J., Thomas, H.J.W., Vasen, H.F., Burn, J., Mathers, J.C.
Published 2015

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

by Burn, J., Gerdes, A.M., Macrae, F., Mecklin, J.P., Moeslein, G., Olschwang, S., Eccles, D., Evans, D.G., Maher, E.R., Bertario, L., Bisgaard, M.L., Dunlop, M.G., Ho, J.W.C., Hodgson, S.V., Lindblom, A., Lubinski, J., Morrison, P.J., Murday, V., Ramesar, R., Side, L., Scott, R.J., Thomas, H.J.W., Vasen, H.F., Barker, G., Crawford, G., Elliott, F., Movahedi, M., Pylvanainen, K., Wijnen, J.T., Fodde, R., Lynch, H.T., Mathers, J.C., Bishop, D.T., CAPP2 Investigators
Published 2011

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

by Mathers, J.C., Movahedi, M., Macrae, F., Mecklin, J.P., Moeslein, G., Olschwang, S., Eccles, D., Evans, G., Maher, E.R., Bertario, L., Bisgaard, M.L., Dunlop, M., Ho, J.W.C., Hodgson, S., Lindblom, A., Lubinski, J., Morrison, P.J., Murday, V., Ramesar, R., Side, L., Scott, R.J., Thomas, H.J.W., Vasen, H., Gerdes, A.M., Barker, G., Crawford, G., Elliott, F., Pylvanainen, K., Wijnen, J., Fodde, R., Lynch, H., Bishop, D.T., Burn, J., CAPP 2 Investigators
Published 2012

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

by Moller, P., Seppala, T., Bernstein, I., Holinski-Feder, E., Sala, P., Evans, D.G., Lindblom, A., Macrae, F., Blanco, I., Sijmons, R., Jeffries, J., Vasen, H., Burn, J., Nakken, S., Hovig, E., Rodland, E.A., Tharmaratnam, K., Cappel, W.H.D.T.N., Hill, J., Wijnen, J., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Renkonen-Sinisalo, L., Frayling, I.M., Plazzer, J.P., Pylvanainen, K., Sampson, J.R., Capella, G., Mecklin, J.P., Moslein, G., Mallorca Grp
Published 2017

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

by Moller, P., Seppala, T., Bernstein, I., Holinski-Feder, E., Sala, P., Evans, D.G., Lindblom, A., Macrae, F., Blanco, I., Jeffries, J., Vasen, H., Burn, J., Nakken, S., Hovig, E., Rodland, E.A., Tharmaratnam, K., Cappel, W.H.D.T.N., Hill, J., Wijnen, J., Jenkins, M., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Renkonen-Sinisalo, L., Frayling, I.M., Plazzer, J.P., Pylvanainen, K., Genuardi, M., Mecklin, J.P., Moslein, G., Sampson, J.R., Capella, G., Mallorca Grp
Published 2017

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

by Seppala, T., Pylvanainen, K., Evans, D.G., Jarvinen, H., Renkonen-Sinisalo, L., Bernstein, I., Holinski-Feder, E., Sala, P., Lindblom, A., Macrae, F., Blanco, I., Sijmons, R., Jeffries, J., Vasen, H., Burn, J., Nakken, S., Hovig, E., Rodland, E.A., Tharmaratnam, K., Cappel, W.H.D.T.N., Hill, J., Wijnen, J., Jenkins, M., Genuardi, M., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Frayling, I.M., Plazzer, J.P., Sampson, J.R., Capella, G., Moslein, G., Mecklin, J.P., Moller, P., Collaboration Mallorca Grp
Published 2017

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

by Thompson, B.A., Spurdle, A.B., Plazzer, J.P., Greenblatt, M.S., Akagi, K., Al-Mulla, F., Bapat, B., Bernstein, I., Capella, G., Dunnen, J.T. den, Sart, D. du, Fabre, A., Farrell, M.P., Farrington, S.M., Frayling, I.M., Frebourg, T., Goldgar, D.E., Heinen, C.D., Holinski-Feder, E., Kohonen-Corish, M., Robinson, K.L., Leung, S.Y., Martins, A., Moller, P., Morak, M., Nystrom, M., Peltomaki, P., Pineda, M., Qi, M., Ramesar, R., Rasmussen, L.J., Royer-Pokora, B., Scott, R.J., Sijmons, R., Tavtigian, S.V., Tops, C.M., Weber, T., Wijnen, J., Woods, M.O., Macrae, F., Genuardi, M., InSiGHT
Published 2014

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

by Moller, P., Seppala, T.T., Bernstein, I., Holinski-Feder, E., Sala, P., Evans, D.G., Lindblom, A., Macrae, F., Blanco, I., Sijmons, R.H., Jeffries, J., Vasen, H.F.A., Burn, J., Nakken, S., Hovig, E., Rodland, E.A., Tharmaratnam, K., Cappel, W.H.D.T.N., Hill, J., Wijnen, J.T., Jenkins, M.A., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Renkonen-Sinisalo, L., Valentin, M.D., Frayling, I.M., Plazzer, J.P., Pylvanainen, K., Genuardi, M., Mecklin, J.P., Moeslein, G., Sampson, J.R., Capella, G., Collaboration Mallorca Grp
Published 2018

The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

by Ahadova, A., Seppala, T.T., Engel, C., Gallon, R., Burn, J., Holinski-Feder, E., Steinke-Lange, V., Moslein, G., Nielsen, M., Broeke, S.W. ten, Laghi, L., Dominguez-Valentin, M., Capella, G., Macrae, F., Scott, R., Huneburg, R., Nattermann, J., Hoffmeister, M., Brenner, H., Blaker, H., Doeberitz, M.V., Sampson, J.R., Vasen, H., Mecklin, J.P., Moller, P., Kloor, M.
Published 2021

Atherothrombosis and Thromboembolism: Position Paper from the Second Maastricht Consensus Conference on Thrombosis

by Spronk, H.M.H., Padro, T., Siland, J.E., Prochaska, J.H., Winters, J., Wal, A.C. van der, Posthuma, J.J., Lowe, G., d'Alessandro, E., Wenzel, P., Coenen, D.M., Reitsma, P.H., Ruf, W., Gorp, R.H. van, Koenen, R.R., Vajen, T., Alshaikh, N.A., Wolberg, A.S., Macrae, F.L., Asquith, N., Heemskerk, J., Heinzmann, A., Moorlag, M., Mackman, N., Meijden, P. van der, Meijers, J.C.M., Heestermans, M., Renne, T., Dolleman, S., Chayoua, W., Ariens, R.A.S., Baaten, C.C., Nagy, M., Kuliopulos, A., Posma, J.J., Harrison, P., Vries, M.J., Crijns, H.J.G.M., Dudink, E.A.M.P., Buller, H.R., Henskens, Y.M.C., Sjalander, A., Zwaveling, S., Erkuner, O., Eikelboom, J.W., Gulpen, A., Peeters, F.E.C.M., Douxfils, J., Olie, R.H., Baglin, T., Leader, A., Schotten, U., Scaf, B., Beusekom, H.M.M. van, Mosnier, L.O., Vorm, L. van der, Declerck, P., Visser, M., Dippel, D.W.J., Strijbis, V.J., Pertiwi, K., Cate-Hoek, A.J. ten, Cate, H. ten
Published 2018